期刊
APPLIED CATALYSIS B-ENVIRONMENTAL
卷 307, 期 -, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.apcatb.2022.121160
关键词
Perovskite; Palladium; Phase boundary; DeNOx catalysis; Reaction kinetics
资金
- special research platform Advanced Materials at the University of Innsbruck
We manipulate the structure and performance of Pd - perovskite interfaces using different preparation methods to achieve optimum NO+CO reactivity in the presence of water. It is found that the extended interface sample aided by H2O can reduce CO poisoning, and the optimized use of lattice oxygen and replenishment from NO dissociation leads to the formation of more poisoning-resistant active sites. Additionally, reaction of species from H2O dissociation with adsorbed CO assists further surface clean off. This study is of great importance for improving catalytic activity and selectivity.
We steer the catalytic performance and morphology of Pd - lanthanum iron manganite (LFM) perovskite interfaces towards optimum NO+CO reactivity in presence of water by following different preparation approaches. Strong CO adsorption for samples without Pd-perovskite interface acts as an inhibitor for adsorption/dissociation of NO, while samples with an extended interface, additionally aided by H2O, show reduced CO poisoning. The optimized use of lattice oxygen for CO oxidation at the phase boundary and its replenishment from NO dissociation allows for the formation of more poisoning-resistant active sites for NO activation. Reaction of species from H2O dissociation with adsorbed CO assists further surface clean off. Enhanced NO reduction activity on the de-poisoned interface leads to a pronounced increase in N-2 selectivity. Preferred production of NH3 at low NO and high CO and H2O concentration indicates that water gas shift intermediates are linked to increased surface hydrogen activity and increased NH3 formation.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据